VHP 136 LOW TEMPERATURE STERILIZATION SYSTEM

VHP 136 LOW TEMPERATURE STERILIZATION SYSTEM is an FDA 510(k)-cleared medical device (K062297) manufactured by STERIS Corporation. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 3, 2007. Regulation: 8.